In this work, the UV-Visible photolysis aqueous ferrioxalate
complexes has been studied kinetically and
mechanistically, in the absence and presence of molecular oxygen.
Catalase enzyme has two functions, first is catalytic and
destroyed with high temperature.
The second function oxidic , increasing with high temperature.
The catalase enzyme effects on the substrate of ortho –
phenylene diamine turning it into ar
omatic cancerogenus azo
compounds
organic acids such as, benzoic acid, salicylic acid and ascorbic
acid inhibit the effect of catalase enzyme substrate ortho –
phenylene diamine. The inhibition is competitive when the
benzoic acid and salicylic acid effects , while the inhibition is
non competitive when the ascorbic acid effect.
Some kinetic parameters have been determined in this work for thermal and catalytic
cracking of the mixed of polyethylene and polypropylene using batch method. The
cracking reaction was carried out at different temperature 470,490 and 510oC under
atmospheric pressure. The mass of products (liquid and gas fractions) were determined and
used to plot the curves of the thermal and catalytic decomposition. We used two types of
catalysts: Syrian natural Zeolite and the same after loading with sulfate ions using
impregnation method. The thermal cracking has a long time and has firs-pseud order
reaction. While in the case of catalytic process we note that the reaction finished in the
short time and the process is the Zero-pseud order reaction. The rate of the cracking
increased very much, the rate constant was k1=0.0032.min-1 in the thermal cracking at
4700C and ko=0.111.min-1 in the case of catalytic cracking in presence of Z catalyst and
ko= 0.206 min-1 in presence of 15-SO4
2-/Z as catalytic at the same temperature. In the other
hand activation energy was 208.7 kj/mol in the thermal process and decreased to 116.6
kj/mol at Z catalytic presence and to 87.3 kj/mol at 15-SO4
2-/Z catalytic presence.
The objective of this study was to study and to analyze caffeine release from gel and
emulgel prepared from carbopol. The properties of the preparations were determined (e.g.
visual inspection, pH test, spreadability and in vitro release). The mech
anisms of caffeine
release were analyzed according to zero and first orders, and to Higuchi and Korsmeyer-
Peppas models. Results were analyzed statistically using student t-test.
The gels were transparent while emulgels were creamy, white and smooth. pH values
were suitable for dermal application and spreadability was not changed in both cases. On
the other hand, accumulated released amount of caffeine was decreased from emulgel in
comparison with the gel. The release pattern was in accordance with Higuchi equation and
n value referred that the diffusion was the main mechanism of release from the gel while
the relaxation and the erosion contributed importantly in the release of suspended caffeine
from emulgel.
Three sampling stations were chosen along the lower reach section of AlSanawbarriver (Lattakia-Syria). In these stations, the freshwater molluscs were studied, environmentally and taxonomically, during the period 4/3/2012 – 4/8/2013.
In this resea
rch, I present the results of the environmental study on the Gastropod Valvatasaulcyiwhich was more abundant in the 3rd station; 5km of the estuary.
Ten mollusc species were identified; 8 belonging to Gastropoda (4 of Prosobranchia & 4 of Pulmonata) and 2 belonging to Bivalvia.
The chemical and physical properties of the water in the 3rd station were studied and the work was concentrated on Valvatasaulcyipopulation and structure, where samples were collected bimonthly during Spring, summer & autumn and monthly during winter. It was shown that reproduction of such species is continuous along the year, with 2 reproduction beaks: the more important one is spring beak and the less important one is autumn beak.
The population structure of the species was studied: shell dimensions were measured and the relationships were studied between height growth and breadth growth of the shell, and between the breadth growth and dry weight of the individual ….
Fattypolyamide was prepared by reaction of (1,5-Diamino pentane) with
dimeric fatty acid C36 in molten state. The reaction was performed at 110 C˚
without catalyst, then with (Phosphoric acid, Sulphoric acid and Manganese
dioxides). The Kinetic st
udy was carried out on the reaction and followed by
determining the acid value of the product. The polyamidation reaction was
found to be on the overall a second order up to 59% conversion. Then the
reaction order changes. We found that the Catalyst increases the velocity of the
reaction with manganese dioxides the best Catalyst. The Degree of
Polymerization, Number Average Molecular Weight and Weight Average
Molecular Weight have been calculated during different times. The
relationships between Degree of Polymerization and Number Average
Molecular Weight, Weight Average Molecular Weight with times are linear
until 59%conversion at 110˚C with used catalysts. The highest (N.A.M.W) and
(W.A.M.W) was accomplished with the Catalyst MnO2.
Study the kinetics degradation of poly (dimeric acid C36 with 1.9 – diamino
nonane) was carried out by thermal analysis (TGA), and thermodynamic and
equilibrium constants have been defined, moreover, study the kinetics of
reaction between 1.9 – di
amino nonane and dimer fatty acid C36 was carried
out in molten state, the reaction was performed at 160 ºC, the acid value, and
percentage of carboxylic functions of the product were determined. The
polyamidation reaction was found to be of overall second order until
conversion of 97% at 160 ºC, then the order of reaction changes.
حركية تفاعل الأميدة
Kinetic of polyamidation reaction
Number Average Molecular Weight
Weight Average Molecular Weight
الحمض الديميري الدسم C36
ثنائيات الأمين
ثوابت ترموديناميكية
الوزن الجزيئي الوسطي العددي
الوزن الجزيئي الوسطي الوزني
الوزن الجزيئي الوسطي اللزوجي
Dimeric fatty acid C36
Diamines
Thermodynamic constants
Viscosity molecular weight
المزيد..
Kinetic studies were carried out on the reaction between dimeric fatty acid
C36 with 1.3 Diamino propane and 1.4 Diamino butane and 1.6 Diamino hexane
and 1.8 Diamino octane in molten phase. The reaction was performed at 145ºC.
The polyamidation r
eaction was found to be on the overall a second order up to
83% conversion for reaction dimeric fatty acid C36 with 1.3 Diamino propane
and 86% conversion for reaction dimeric fatty acid C36 with 1.4 Diamino
butane and 87% conversion for reaction dimeric fatty acid C36 with 1.6
Diamino hexane and 1.8 Diamino octane then the reaction order changes to the
third order above last conversion. The degree of polymerization,number
average molecular weight and weight average molecular weight have been
calculated during different times. Their relationships with the times are linear
until last conversion. The melting point and thermodynamic constants for
melting are determined by use of differential scanning calorimetry DSC. The
melting point and thermodynamic constants increase by increasing the length
of reacted amine series.
Kinetic studies were carried out on the reaction between 1,10–
Decanedioland dimeric fatty acid C36 in melt phase. The reaction was
performed at 140, 150, 160, 170, and 185ºC and followed by determining the
acid value of the product.
Kinetic studies were carried out on the reaction between 2-Methyl 1,5
diaminopentane and dimeric fatty acids in melt phase. The reaction was
performed at 113, 130, 140, 155, and 164 ºC and followed by determining the
acid value of the product .The
polyamidation reaction was found to be of
overall second order with an activation energy of 45.48 k cal⁄g mol up to (52, 57,
79, 80, 86)% conversion at (113, 130, 140, 155, 164) ºC and overall third order
with an activation energy of 43.73 k cal⁄g mol above (52, 57, 79, 80, 86)%
conversion at (113, 130, 140, 155, 164) ºC.